Search
Descriptor English: Myeloproliferative Disorders
Descriptor Spanish: Trastornos Mieloproliferativos
Descriptor trastornos mieloproliferativos
Scope note: Afecciones que causan proliferación de tejidos con actividad hematopoyética o de tejidos que poseen potencial embrionario hematopoyético. Todas ellas producen alteraciones en la regulación de las CÉLULAS PROGENITORAS MIELOIDES, muy frecuentemente por causa de una mutación en la PROTEINA TIROSINA QUINASA JAK2.
Descriptor Portuguese: Transtornos Mieloproliferativos
Descriptor French: Syndromes myéloprolifératifs
Entry term(s): Disorder, Myeloproliferative
Disorders, Myeloproliferative
Myeloproliferative Disorder
Tree number(s): C15.378.190.636
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D009196
Scope note: Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE.
Annotation: myelo- here = bone marrow, not spinal cord; general; prefer specifics
Allowable Qualifiers: BL blood
CF cerebrospinal fluid
CI chemically induced
CL classification
CN congenital
CO complications
DG diagnostic imaging
DH diet therapy
DI diagnosis
DT drug therapy
EC economics
EH ethnology
EM embryology
EN enzymology
EP epidemiology
ET etiology
GE genetics
HI history
IM immunology
ME metabolism
MI microbiology
MO mortality
NU nursing
PA pathology
PC prevention & control
PP physiopathology
PS parasitology
PX psychology
RH rehabilitation
RT radiotherapy
SU surgery
TH therapy
UR urine
VE veterinary
VI virology
Public MeSH Note: 70
History Note: 70(66)
Entry Version: MYELOPROLIFERATIVE DIS
Related: Leukemia MeSH
DeCS ID: 9388
Unique ID: D009196
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1970/01/01
Date of Entry: 1999/01/01
Revision Date: 2007/07/09
Myeloproliferative Disorders - Preferred
Concept UI M0014332
Scope note Conditions which cause proliferation of hemopoietically active tissue or of tissue which has embryonic hemopoietic potential. They all involve dysregulation of multipotent MYELOID PROGENITOR CELLS, most often caused by a mutation in the JAK2 PROTEIN TYROSINE KINASE.
Preferred term Myeloproliferative Disorders
Entry term(s) Disorder, Myeloproliferative
Disorders, Myeloproliferative
Myeloproliferative Disorder



We want your feedback on the new DeCS / MeSH website

We invite you to complete a survey that will take no more than 3 minutes.

Go to survey